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Lipids of cultured hepatoma cells: VI. Glycerolipid and monoenoic fatty acid biosynthesis in minimal deviation hepatoma 7288C

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Lipids

Abstract

1-14C-Acetic, 1-14C-palmitic, or 1-14C-stearic acid was incubated with minimal deviation hepatoma 7288C cells grown in culture to assess: de novo fatty acid synthesis, oxidation, desaturation, and elongation of saturated fatty acids, as well as the ability of media fatty acids to serve as precursors of cellular glycerolipids. Distribution of radioactivity in the individual lipid classes and the various fatty acids of triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine was determined. The radioactivity among the monoenoic acid isomers derived from triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine was analyzed by reductive ozonolysis. Only small amounts of the labeled substrates were oxidized to carbon dioxide. Except for labeled stearic acid, which also was incorporated heavily into phosphatidyl inositol and phosphatidyl serine, most radioactivity was recovered in triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine. Synthesis of cholesterol and long chain fatty acids from labeled acetic acid demonstrated that these cells can perform de novo synthesis of fatty acids and cholesterol. Both labeled palmitic and stearic acids were desaturated to the corresponding Δ9 monoenes, and palmitic and palmitoleic acids were elongated. The hexadecenoic acid fraction isolated from triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine, when acetic or palmitic acid was the labeled substrate, showed that greater than 70% of the labeled acids were the Δ9 isomer. Radioactivity of the octadecenoic acid fraction derived from labeled acetic or palmitic acids was nearly equally divided between the Δ9 isomer, oleic acid, and the Δ11 isomer, vaccenic acid. Desaturation of labeled stearic acid produced only oleic acid. These data demonstrate that the biosynthesis of vaccenic acid in these cultured neoplastic cells proceeds via the elongation of palmitoleic acid. The relatively high level of vaccenic acid synthesis in these cells suggests that the reported elevation of “oleic acid” in many neoplasms may result from increased concentration of vaccenic acid.

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References

  1. Wood, R., Lipids 8:690 (1973).

    Article  PubMed  CAS  Google Scholar 

  2. Wiegand, R.D., and R. Wood, Lipids 9:141 (1974).

    PubMed  CAS  Google Scholar 

  3. Watson, J.A., in “Tumor Lipids: Biochemistry and Metabolism,” Edited by Randall Wood, AOCS, Champaign, Ill., 1973, p. 34.

    Google Scholar 

  4. Avigan, J., C.D. Williams, and J.P. Blass, Biochim. Biophys. Acta 125:226 (1966).

    Google Scholar 

  5. Bligh, E.G., and W.J. Dyer, Can. J. Biochem. Physiol. 37:911 (1959).

    PubMed  CAS  Google Scholar 

  6. Bergstrom, B., Acta Physiol. Scand. 25:101 (1952).

    Article  Google Scholar 

  7. Beroza, M., and B.A. Bierl, Anal. Chem. 39:1131 (1967).

    Article  CAS  Google Scholar 

  8. Wood, R., and R. Reiser, JAOCS 42:159 (1965).

    CAS  Google Scholar 

  9. Wood, R., and K. Healy, J. Biol. Chem. 245:2640 (1970).

    PubMed  CAS  Google Scholar 

  10. Wood, R., and J. Falch, Lipids 8:702 (1973).

    Article  PubMed  CAS  Google Scholar 

  11. Wood, R., and J. Falch, Ibid. 9:979 (1974).

    PubMed  CAS  Google Scholar 

  12. Holloway, P.W., and S.J. Wakil, J. Biol. Chem. 239:2489 (1964).

    PubMed  CAS  Google Scholar 

  13. Elovson, J., Biochim. Biophys. Acta 106:291 (1965).

    PubMed  CAS  Google Scholar 

  14. Weinhouse, S., J. Langan, J.A. Shatton, and H.P. Morris, in “Tumor Lipids: Biochemistry and Metabolism,” Edited by Randall Wood, AOCS, Champaign, Ill., 1973, p. 4.

    Google Scholar 

  15. Sabine, J.R., Ibid. p.21.

    Google Scholar 

  16. Watson, J.A., E.S. Kirsten, and J.B. Quint, Fed. Proc. 33:1573 (1974).

    Google Scholar 

  17. Geyer, R.P., in “Lipid Metabolism in Tissue Culture Cells,” Edited by G.H. Rothblat and D. Kritchevsky, Monograph 6, Wistar Institute Symposium, Wistar Press, Philadelphia, Pa., 1967, p. 33.

    Google Scholar 

  18. Moskowitz, M.S., Ibid. in “, p. 49.

    Google Scholar 

  19. Mackenzie, C.G., J.B. Mackenzie, and O.K. Reiss, Ibid. in “, p. 63.

    Google Scholar 

  20. Bailey, J.M., B.V. Howard, and S.G. Tillman, J. Biol. Chem. 248:1240 (1973).

    PubMed  CAS  Google Scholar 

  21. Stoffel, W., and A. Scheid, Z. Physiol. Chem. 348:205 (1967).

    CAS  Google Scholar 

  22. Spector, A.A., in “Growth, Nutrition, and Metabolism of Cells in Culture,” Vol. 1, Eidited by G.H. Rothblat and V.J. Cristofalo, Academic Press, New York, N.Y., 1972, p. 257.

    Google Scholar 

  23. Wood, R., J. Falch, and R.D. Wiegand, Lipids 9:987 (1974).

    PubMed  CAS  Google Scholar 

  24. Ruggieri, S., and A. Fallani, in “Tumor Lipids: Biochemistry and Metabolism,” Edited by Randall Wood, AOCS, Champaign, Ill., 1973, p. 89.

    Google Scholar 

  25. Bergelson, L.D., and E.V. Dyatlovitskaya, Ibid. in “, p. 111.

    Google Scholar 

  26. van Hoeven, R.P., and P. Emmelot, Ibid. in “, p. 126.

    Google Scholar 

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Wiegand, R.D., Wood, R. Lipids of cultured hepatoma cells: VI. Glycerolipid and monoenoic fatty acid biosynthesis in minimal deviation hepatoma 7288C. Lipids 10, 194–201 (1975). https://doi.org/10.1007/BF02534159

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  • DOI: https://doi.org/10.1007/BF02534159

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